Details of Disease | DrugMAP

General Information of Disease (ID: DISNRVHK)

Disease Name	Ovarian dysgenesis 7
Synonyms	ODG7; OVARIAN DYSGENESIS 7
Disease Hierarchy	DISBB9HA: 46 XX gonadal dysgenesis DISNRVHK: Ovarian dysgenesis 7
Disease Identifiers	MONDO ID MONDO_0020857 UMLS CUI C4748263 OMIM ID 618117 MedGen ID 1648458

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)

This Disease Is Related to 1 DOT Molecule(s)

Gene Name	DOT ID	Evidence Level	Mode of Inheritance	REF
MRPS22	OTIVNAJL	Limited	Autosomal recessive	[1]
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References

1	Mutations in the mitochondrial ribosomal protein MRPS22 lead to primary ovarian insufficiency. Hum Mol Genet. 2018 Jun 1;27(11):1913-1926. doi: 10.1093/hmg/ddy098.